Canonical Allele Identifier: CA2014120730

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534730A= , CM000674.2:g.6534730A=	GRCh38
NC_000012.11:g.6643896A= , CM000674.1:g.6643896A=	GRCh37
NC_000012.10:g.6514157A=	NCBI36
NG_007073.2:g.5240A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.-23-80A= MANE Select	ENSP00000229239.5:n.-23-80A=
ENST00000229239.9:c.-23-80A=	ENSP00000229239.5:n.-23-80A=
ENST00000396856.5:c.-275-80A=	ENSP00000380065.1:n.-275-80A=
ENST00000396861.5:c.-24+69A=	ENSP00000380070.1:n.-24+69A=
ENST00000474249.5:n.30-80A=
ENST00000492719.5:n.38-80A=
ENST00000496049.1:n.59-80A=
NM_001289745.1:c.-24+69A=	NP_001276674.1:n.-24+69A=
NM_001289746.1:c.-103A=	NP_001276675.1:n.-103A=
NM_002046.5:c.-23-80A=	NP_002037.2:n.-23-80A=
NM_001289745.2:c.-24+69A=	NP_001276674.1:n.-24+69A=
NM_001357943.1:c.-23-80A=	NP_001344872.1:n.-23-80A=
NM_002046.6:c.-23-80A=	NP_002037.2:n.-23-80A=
NR_152150.1:n.54-80A=
NM_002046.7:c.-23-80A= MANE Select	NP_002037.2:n.-23-80A=
NM_001289745.3:c.-24+69A=	NP_001276674.1:n.-24+69A=
NM_001289746.2:c.-103A=	NP_001276675.1:n.-103A=
NM_001357943.2:c.-23-80A=	NP_001344872.1:n.-23-80A=
NR_152150.2:n.54-80A=